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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

Boronic acid, [2-formyl-4-(phenylmethoxy)phenyl]-

O=Cc1cc(OCc2ccccc2)ccc1B(O)O Request for Quotation
Chemical Name: Boronic acid, [2-formyl-4-(phenylmethoxy)phenyl]-
CAS Number: 139962-97-3
Product Number: AG001BVA(AGN-PC-0L0N1U)
Synonyms:
MDL No:
Molecular Formula: C14H13BO4
Molecular Weight: 256.0616

Identification/Properties

Computed Properties
Molecular Weight:
256.064g/mol
Hydrogen Bond Donor Count:
2
Hydrogen Bond Acceptor Count:
4
Rotatable Bond Count:
5
Exact Mass:
256.091g/mol
Monoisotopic Mass:
256.091g/mol
Topological Polar Surface Area:
66.8A^2
Heavy Atom Count:
19
Formal Charge:
0
Complexity:
279
Isotope Atom Count:
0
Defined Atom Stereocenter Count:
0
Undefined Atom Stereocenter Count:
0
Defined Bond Stereocenter Count:
0
Undefined Bond Stereocenter Count:
0
Covalently-Bonded Unit Count:
1
Compound Is Canonicalized:
Yes

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


(4-(Benzyloxy)-2-formylphenyl)boronic acid is a versatile compound commonly employed in chemical synthesis processes. This boronic acid derivative is frequently utilized as a key building block in the construction of various organic molecules due to its unique reactivity and functional groups. In organic synthesis, this compound serves as a valuable precursor for the introduction of the phenylboronic acid moiety into diverse target molecules.One prominent application of (4-(Benzyloxy)-2-formylphenyl)boronic acid is its role as a valuable reagent in Suzuki-Miyaura cross-coupling reactions. This powerful synthetic method involves the coupling of an aryl or heteroaryl boronic acid with an organic halide or pseudohalide, catalyzed by a palladium catalyst. By utilizing (4-(Benzyloxy)-2-formylphenyl)boronic acid as one of the coupling partners, chemists can efficiently introduce the phenylboronic acid functionality into complex molecules, enabling the synthesis of structurally diverse compounds.Furthermore, (4-(Benzyloxy)-2-formylphenyl)boronic acid can also participate in other important transformations such as direct arylation reactions, boronate ester formation, and C-H activation processes. Its versatile reactivity and compatibility with various reaction conditions make it a valuable tool for the construction of pharmaceuticals, agrochemicals, and materials with tailored properties.Overall, the strategic incorporation of (4-(Benzyloxy)-2-formylphenyl)boronic acid in chemical synthesis enables researchers to access novel molecular architectures and functionalized compounds with potential applications in drug discovery, materials science, and beyond.